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Details
Link-It Detail - Disease - Retinal Detachment
Debug Stats
  • ### Total Build Time: 38 ms 34.100 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 334 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 506 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 552 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.492 KB
  • CONCEPT_RELATIONSHIPS gt=23 ms Completed: 23 ms rowSize= 13.669 KB
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 16.208 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.152 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Retinal Detachment C0035305
Definition (1)
An eye emergency condition which may lead to blindness if left untreated. It is characterized by the separation of the inner retina layers from the underlying pigment epithelium. Causes include trauma, advanced diabetes mellitus, high myopia, and choroid tumors. Symptoms include sudden appearance of floaters, sudden light flushes, and blurred vision.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Retinal Diseases C0035309
Ancestral Roots
RootRoot Plus OneDepthParent
img Eye Diseases C0015397img Retinal Diseases C00353093img Retinal Diseases C0035309
Relationships (95)

Relation Types:
diso_​to_​anat : 18
diso_​to_​chem : 7
diso_​to_​diso : 67
diso_​to_​phen : 1
diso_​to_​phys : 2


Relationships:
none : 62
classifies : 2
expanded_​form_​of : 1
is_​associated_​anatomic_​site_​of : 2
isa : 19
mapped_​to : 8
parent_​is_​cdrh : 1
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO180img Retinal Perforations C0035321
DISO_to_DISO168img Complication Aspects C1171258
DISO_to_DISO128img Retinal Perforations C0035321
DISO_to_CHEM101img SILICONE OIL C0037111
DISO_to_DISO101img Complication Aspects C1171258
DISO_to_ANAT97img Retina C0035298
DISO_to_DISO92img COMPL POSTOP C0032787
DISO_to_DISO89img COMPL POSTOP C0032787
DISO_to_DISO83img Proliferative vitreoretinopathy C0242852
DISO_to_ANAT64img Retina C0035298
DISO_to_CHEM64img SILICONE OIL C0037111
DISO_to_ANAT56img Macula Lutea C0450295
DISO_to_ANAT56img Retinal Pigment Epithelium C0035322
DISO_to_CHEM55img ANGIOGENESIS INHIB C0596087
DISO_to_CHEM55img Antibodies, Monoclonal C0003250
DISO_to_ANAT53img Vitreous Body C0042905
DISO_to_ANAT50img Eye Pigment Epithelium C0031907
DISO_to_DISO50img Myopia C0027092
DISO_to_ANAT48img Macula Lutea C0450295
DISO_to_CHEM48img Fluorocarbons C0016340
DISO_to_DISO48img Age related macular degeneration C0242383
DISO_to_PHYS48img Visual Acuity C0042812
DISO_to_DISO46img Diabetic Retinopathy C0011884
DISO_to_DISO46img Proliferative vitreoretinopathy C0242852
DISO_to_PHYS44img Visual Acuity C0042812
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanCOL18A180781collagen, type XVIII, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanFKRP79147fukutin related protein
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanPOMT229954protein-O-mannosyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanPOMT110585protein-O-mannosyltransferase 1
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanLARGE9215like-glycosyltransferase
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanCCL26347chemokine (C-C motif) ligand 2
img GENERIF, Score=673, Pubmed Id: 17284607, UMLKSK CUI: C0035305
HumanPLOD15351procollagen-lysine, 2-oxoglutarate 5-dioxygenase 1
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanPAX65080paired box 6
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanNPY1R4886neuropeptide Y receptor Y1
img GENERIF, Score=861, Pubmed Id: 12203398, UMLKSK CUI: C0035305
HumanNDP4693Norrie disease (pseudoglioma)
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanLRP24036low density lipoprotein receptor-related protein 2
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanFKTN2218fukutin
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanFBN12200fibrillin 1
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanCOL11A11301collagen, type XI, alpha 1
img OMIM, Score=1000, UMLKSK CUI: C0035305
HumanCOL2A11280collagen, type II, alpha 1
img GENERIF, Score=1000, Pubmed Id: 14644246, UMLKSK CUI: C0035305
img OMIM, Score=1000, UMLKSK CUI: C0035305
img GAD, Score=1000, Pubmed Id: 12939326, UMLKSK CUI: C0035305
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0035305Retinal Detachment0self